可解释性
计算机科学
机器学习
水准点(测量)
人工智能
过程(计算)
药物开发
相互信息
药物发现
保险丝(电气)
机制(生物学)
药物靶点
标记数据
数据挖掘
药品
生物信息学
工程类
药理学
大地测量学
电气工程
操作系统
生物
地理
医学
哲学
认识论
作者
Shuting Xu,Ruochen Wang
标识
DOI:10.1109/ictai59109.2023.00106
摘要
Accurate and effective Drug Target binding Affinity (DTA) prediction can significantly shorten the drug development lifecycle and reduce the cost. Although many deep learning-based methods have been developed for DTA prediction, most do not model complex drug-target interaction process and have poor interpretability. In addition, these models depend on large-scale labelled data. To address these problems, we designed a new DTA prediction model called OdinDTA. We use drug sequences and graphs to extract drug features in this model. To meet the challenge of labelled data scarcity, our studies adopted self-supervised pre-training tasks to learn information of amino acid sequences of proteins. Finally, we utilize the mutual attention mechanism to fuse the representations of drugs and proteins. We evaluate the performance of our method on two benchmark datasets, KIBA and Davis. Experimental results show that our model outperforms the current state-of-the-art methods on two independent datasets.
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